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Zilver Flex Post-Market Study in Japan

NCT02254356 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 239

Last updated 2018-03-30

No results posted yet for this study

Summary

Japanese post market clinical study of the Zilver Flex device.

Conditions

  • Peripheral Arterial Disease (PAD)

Interventions

DEVICE

Zilver Flex Bare Metal Stent

Sponsors & Collaborators

  • Cook Group Incorporated

    lead INDUSTRY

Principal Investigators

  • Michael D Dake, MD · Department of Cardiothoracic Surgery, Stanford University Medical Center, Stanford, CA

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-05-31
Primary Completion
2017-12-26
Completion
2017-12-26

Countries

  • Japan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02254356 on ClinicalTrials.gov